Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis
Ticozzi, N., Vance, C., LeClerc, A.L., Keagle, P., Glass, J.D., McKenna-Yasek, D., Sapp, P.C., Silani, V., Bosco, D.A., Shaw, C.E., Brown Jr, R.H., Landers, J.E.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2011)
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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr
Published in Science (American Association for the Advancement of Science) (27.02.2009)
Published in Science (American Association for the Advancement of Science) (27.02.2009)
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SOD1 A4V-mediated ALS: Absence of a closely linked modifier gene and origination in Asia
Broom, W.J., Johnson, D.V., Auwarter, K.E., Iafrate, A.J., Russ, C., Al-Chalabi, A., Sapp, P.C., McKenna-Yasek, D., Andersen, P.M., Brown, R.H.
Published in Neuroscience letters (2008)
Published in Neuroscience letters (2008)
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SOD1A4V-mediated ALS : Absence of a closely linked modifier gene and origination in Asia
BROOM, W. J, JOHNSON, D. V, AUWARTER, K. E, IAFRATE, A. J, RUSS, C, AL-CHALABI, A, SAPP, P. C, MCKENNA-YASEK, D, ANDERSEN, P. M, BROWN, R. H
Published in Neuroscience letters (17.01.2008)
Published in Neuroscience letters (17.01.2008)
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Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1
Rosen, D R, Sapp, P C, O'Regan, J, Horvitz, H R, Donaldson, D H, Nussbaum, C, Gusella, J F, Haines, J L, Pestka, S, Jung, V
Published in Human molecular genetics (01.10.1992)
Published in Human molecular genetics (01.10.1992)
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